Use Risk Assessment to Reduce Validation Time for 21 CFR Part 11 2015

  • 10 Apr 2015
  • Webinar

Description

Topics
  • Step-by-step instructions for performing and documenting a risk assessment
  • How to use the risk-based approach to reduce validation time and lower costs
  • Avoid 483s and Warning Letters
  • How to use the results to reduce testing requirements
  • How to identify risk in a process and establish mitigations to reduce liability
Who should Attend
  • IT personnel
  • Computer system users
  • Managers
  • QA personnel
  • Executives

Past Events

Important

Please, check "Use Risk Assessment to Reduce Validation Time for 21 CFR Part 11" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Pharma
Technology: Information Technology (IT)

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